... RAVE EDC, DS Navigator, SAS Programming, Reporting and Analytics, Siebel CTMS, Documentum ... Medidata CTMS, BioClinica CTMS, ArisGlobal CTMS) 3) eTMF Solutions (i.e. VEEVA, Documentum ...
... RAVE EDC, DS Navigator, SAS Programming, Reporting and Analytics, Siebel CTMS, Documentum ... Medidata CTMS, BioClinica CTMS, ArisGlobal CTMS) 3) eTMF Solutions (i.e. VEEVA, Documentum ...
Bachelor's degree in Life Sciences, Computer Science, Engineering, Information Systems, Data ... Experience with Rave Medidata or similar EDC platforms * Experience integrating IxRS and EDC ...
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Bachelor's degree in Life Sciences, Computer Science, Engineering, Information Systems, Data ... Experience with Rave Medidata or similar EDC platforms * Experience integrating IxRS and EDC ...
Internship Medidata Rave Programmer information
What does an Internship Medidata Rave Programmer do?
An Internship Medidata Rave Programmer assists in designing, developing, and maintaining electronic data capture (EDC) systems using Medidata Rave for clinical trials. Their main tasks include programming study databases, building case report forms (CRFs), and ensuring data quality and compliance with regulatory standards. Interns typically work under the supervision of experienced programmers and may also help troubleshoot technical issues, support data validation, and learn about clinical data management processes. This role provides hands-on experience with clinical trial technology and helps interns build foundational skills for a future career in clinical data programming.
What are some typical projects or tasks an Internship Medidata Rave Programmer might work on?
As an Internship Medidata Rave Programmer, you can expect to assist with building and maintaining electronic case report forms (eCRFs), validating study configurations, and supporting data management teams in clinical trials. You may also help troubleshoot and resolve issues within Medidata Rave, perform quality checks, and contribute to documentation. Collaboration with experienced programmers and data managers is common, providing valuable exposure to real-world clinical data workflows and industry best practices.
What is the difference between Internship Medidata Rave Programmer vs Clinical Data Coordinator?
| Aspect | Internship Medidata Rave Programmer | Clinical Data Coordinator |
|---|---|---|
| Required Credentials | Basic knowledge of Medidata Rave, relevant coursework or certifications | Degree in life sciences, healthcare, or related field; often additional certifications |
| Work Environment | Internship setting, often in pharmaceutical or biotech companies | Clinical trial sites or sponsor organizations, managing data entry and quality |
| Industry Usage | Used primarily in clinical data management and EDC system setup | Used in clinical trial data collection, management, and compliance |
The Internship Medidata Rave Programmer typically focuses on learning and supporting EDC system setup and data management using Medidata Rave, often as part of an internship program. In contrast, a Clinical Data Coordinator manages data collection, quality control, and compliance during clinical trials. Both roles are essential in clinical research but differ in responsibilities and experience levels.
What are the key skills and qualifications needed to thrive as an Internship Medidata Rave Programmer, and why are they important?
To thrive as an Internship Medidata Rave Programmer, you need a solid background in computer science or life sciences, familiarity with clinical data management concepts, and basic programming skills. Experience with Medidata Rave EDC platform, clinical trial management systems, and understanding of CDISC standards or certifications like Medidata Rave certification are valuable. Attention to detail, problem-solving abilities, and strong communication skills help you collaborate effectively with clinical teams and ensure data integrity. These skills are essential for supporting efficient, compliant data capture and management in clinical research environments.
What are the most commonly searched types of Medidata Rave Programmer jobs in California? The most popular types of Medidata Rave Programmer jobs in California are:
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Other
Medical, Dental, Vision, Life, Retirement, PTO
Posted 14 days ago
Job description
Company Description
About Collabera:
Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion dollar IT company, Collabera's client-centric business model, commitment to service excellence and Global Delivery Model enables its global 2000 and leading mid-market clients to deliver successfully in an increasingly competitive marketplace.
With over 8200 IT professionals globally, Collabera provides value-added onsite, offsite and offshore technology services and solutions to premier corporations. Over the past few years, Collabera has been awarded numerous accolades and Industry recognitions including.
Collabera awarded Best Staffing Company to work for in 2012 by SIA. (hyperlink here)
Collabera listed in GS 100 - recognized for excellence and maturity
Collabera named among the Top 500 Diversity Owned Businesses
Collabera listed in GS 100 & ranked among top 10 service providers
Collabera was ranked:
32 in the Top 100 Large Businesses in the U.S
18 in Top 500 Diversity Owned Businesses in the U.S
3 in the Top 100 Diversity Owned Businesses in New Jersey
3 in the Top 100 Privately-held Businesses in New Jersey
66th on FinTech 100
35th among top private companies in New Jersey
http://www.collabera.com/about_us/accolades.jsp
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.
Job Description
Job Description for Clinical Solutions Project Manager - Contract position
Oversight and management of Clinical Trial systems used by Clinical Research organization
Program and Project Management for Clinical Systems projects including system updates, enhancements, and new system implementation
Author project documentation including Project Charters, Business Requirements etc...
Develop and present Clinical System strategies and roadmaps.
Partner with global Clinical Research functions to identify business needs and propose new/enhance existing clinical system solutions.
Drive adoption of and facilitate change management of clinical systems in the global Clinical Research function
Develop and Conduct clinical systems training for Global Business End Users
Manage System Vendor relationships.
Provide global production support activities
Skills - Program Management, Project Management, Technology Strategy, SDLC, Business Process Modeling, Vendor Management, User Adoption, System Training, Business Analysis
Clinical Research Functional Experience - Data Management, Clinical Safety, Biostatistics
Systems Experience - RAVE EDC, DS Navigator, SAS Programming, Reporting and Analytics, Siebel CTMS, Documentum
Qualifications
equirements
BA or BS degree in technical or scientific discipline required.
8+ years of experience implementing systems in GxP controlled environment including responsibility for the implementation of either an EDC, Safety or CTMS system.
Strong interpersonal and communication skills; ability to interact with different levels of management.
Experience with implementation of CTMS tool highly desired.
Clinical Research experience in the Medical Device/Pharma industry is a plus.
Skills
1) Project Management
2) Business Analysis
3) Business Process Modeling
4) Clinical Technology Strategy
5) User Adoption
6) System Training
7) Vendor Management
Systems Experience
1) RAVE EDC
2) CTMS (preferably Oracle CTMS, Medidata CTMS, BioClinica CTMS, ArisGlobal CTMS)
3) eTMF Solutions (i.e. VEEVA, Documentum, NextDocs)
4) Safety Database
5) Reporting and Analytics
6) DS Navigator
7) SAS Programming
Additional Information
All your information will be kept confidential according to EEO guidelines.